Literature DB >> 11677629

Identifications, classification, and evolution of the vertebrate alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptor subunit genes.

Y C Chen1, S S Kung, B Y Chen, C C Hung, C C Chen, T Y Wang, Y M Wu, W H Lin, C S Tzeng, W Y Chow.   

Abstract

The AMPA receptor (AMPAR), a pharmacologically defined ionotropic glutamate receptor, mediates fast excitatory synaptic transmission in the vertebrate central nervous system. Mammalian and avian AMPARs are assembled from the products of four genes (GRIA1-GRIA4) conserved in their translated sequences and gene organizations. Teleost fish also express AMPAR subunits; however, the AMPAR genes have not been extensively investigated in lower vertebrates. To elucidate the evolution of vertebrate AMPAR genes, reverse-transcriptase PCR-based surveys of subunits expressed in the brains of eight nonmammalian vertebrates were performed. The newly cloned vertebrate AMPAR subunits were classified by their sequence identities to the mammalian AMPAR subunits. The results of molecular and phylogenetic analyses indicated that the members of the AMPAR gene family increased from two in the jawless hagfish to four in the tetrapods and the shark and to more than four in the teleost fish. The sizes of AMPAR gene families correlate well with those of many multigene families observed in various vertebrates. Moreover, all vertebrates expressed at least one AMPAR subunit bearing an arginine (R) at the Q/R site, at which no invertebrate glutamate receptor subunit has been found to have an R residue, suggesting that the low calcium-permeable AMPARs appeared at early evolutionary stages of vertebrate central nervous systems. Uniquely, the loop 1 (L1) regions between hydrophobic domain 1 and hydrophobic domain 2 of the hagfish putative GRIA2 and all the teleost GRIA1 subunits were much longer than those of the remaining known ionotropic glutamate receptor subunits. The length and sequence of the L1 of teleost GRIA1 subunits were heterogeneous, suggesting that the amino acid residues in L1 were not highly selected.

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Year:  2001        PMID: 11677629     DOI: 10.1007/s002390010256

Source DB:  PubMed          Journal:  J Mol Evol        ISSN: 0022-2844            Impact factor:   2.395


  6 in total

1.  The mutually exclusive flip and flop exons of AMPA receptor genes were derived from an intragenic duplication in the vertebrate lineage.

Authors:  Yu-Chia Chen; Wei-Hsiang Lin; Der-Wang Tzeng; Wei-Yuan Chow
Journal:  J Mol Evol       Date:  2006-01-13       Impact factor: 2.395

Review 2.  The role of AMPA receptor modulation in the treatment of neuropsychiatric diseases.

Authors:  Carlos A Zarate; Husseini K Manji
Journal:  Exp Neurol       Date:  2008-01-26       Impact factor: 5.330

3.  AMPA glutamate receptors are required for sensory-organ formation and morphogenesis in the basal chordate.

Authors:  Shinobu Hirai; Kohji Hotta; Yoshihiro Kubo; Atsuo Nishino; Shigeo Okabe; Yasushi Okamura; Haruo Okado
Journal:  Proc Natl Acad Sci U S A       Date:  2017-03-27       Impact factor: 11.205

4.  Dynamic Changes in Synaptic Plasticity Genes in Ipsilateral and Contralateral Inferior Colliculus Following Unilateral Noise-induced Hearing Loss.

Authors:  Senthilvelan Manohar; Francesca Yoshie Russo; Gail M Seigel; Richard Salvi
Journal:  Neuroscience       Date:  2020-04-09       Impact factor: 3.590

5.  Habitat Partitioning and its Possible Genetic Background Between Two Sympatrically Distributed Eel Species in Taiwan.

Authors:  Hsiang-Yi Hsu; Hsiao-Wei Chen; Yu-San Han
Journal:  Zool Stud       Date:  2019-09-18       Impact factor: 2.058

6.  Aestivation and hypoxia-related events share common silent neuron trafficking processes.

Authors:  Giuseppina Giusi; Merylin Zizza; Rosa Maria Facciolo; Shit Fun Chew; Yuen Kwong Ip; Marcello Canonaco
Journal:  BMC Neurosci       Date:  2012-04-20       Impact factor: 3.288

  6 in total

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